Identity
- Trade Name
- 6991 ANASTHESIA FACE MASK FDA UDI
- Generic Name
- Anaesthesia face mask, reusable FDA UDI
- Device Name
- ANESTHESIA MASK ADULT SM 22MM FDA UDI
- Model / Reference
- 6991 FDA UDI
- Description
- ANESTHESIA MASK ADULT SM 22MM FDA UDI
Identifiers
- Catalog Number
- 669058 FDA UDI
- Primary DI / UDI-DI
- 00874750005857 FDA UDI
- FDA Product Code
- BSJ FDA UDI
- GMDN Term
- Anaesthesia face mask, reusable FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 868.5550 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
6991 Anasthesia Face Mask by Hans Rudolph, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Hans Rudolph, Inc.
Sources (1)
- FDA UDI d7c61ef2-e3cb-4238-948c-c42d5e6528e1 35 fields · synced Jun 8, 2026